The RNA-guided endonuclease Cas9 can be converted into a programmable transcriptional repressor. Here we describe a set of protocols for using the catalytically inactive dead Cas9 (dCas9)-based tools, including the bipartite super repressor consisting of the KRAB and MeCP2 domains, to achieve efficient and scalable gene silencing in mammalian cells.
Keywords: CRISPR-Cas transcriptional repressor; Single and multiplex gene silencing; dCas9-KRAB-MeCP2.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.